Differential inhibition of Smad6 and Smad7 on bone morphogenetic protein- and activin-mediated growth arrest and apoptosis in B cells

被引:195
作者
Ishisaki, A
Yamato, K
Hashimoto, S
Nakao, A
Tamaki, K
Nonaka, K
ten Dijke, P
Sugino, H
Nishihara, T
机构
[1] Nstl Inst Infect Dis, Dept Oral Sci, Shinjuku Ku, Tokyo 1628640, Japan
[2] Tokyo Med & Dent Univ, Fac Dent, Dept Mol Cellular Oncol Microbiol, Bunkyo Ku, Tokyo 1138549, Japan
[3] Tokyo Med & Dent Univ, Fac Dent, Dept Oral & Maxillofacial Surg 1, Bunkyo Ku, Tokyo 1138549, Japan
[4] Chiba Univ, Sch Med, Dept Med, Chuo Ku, Chiba 2600856, Japan
[5] Univ Tokushima, Inst Enzyme Res, Tokushima 770, Japan
[6] Biomed Ctr, Ludwig Inst Canc Res, S-75124 Uppsala, Sweden
关键词
D O I
10.1074/jbc.274.19.13637
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Smad6 and Smad7 prevent ligand-induced activation of signal-transducing Smad proteins in the transforming growth factor-p family. Here we demonstrate that both Smad6 and Smad7 are human bone morphogenetic protein-2 (hBMP-2)-inducible antagonists of hBMP-2-induced growth arrest and apoptosis in mouse B cell hybridoma HS-72 cells. Moreover, we confirmed that the ectopic expressions of Smad6 and Smad7 inhibited the hBMP-2-induced Smad1/Smad5 phosphorylation. We previously reported that Smad7 is an activin A-inducible antagonist of activin A-induced growth arrest and apoptosis in HS-72 cells. Interestingly, although mRNA expression of Smad6 was induced by activin A in HS-72 cells, Smad6 showed no antagonistic effect on activin A-induced growth arrest and apoptosis, Moreover, we found that the ectopic expression of Smad7, but not Smad6, inhibited the activin A-induced Smad2 phosphorylation in HS-72 cells. Thus, Smad6 and Smad7 exhibit differential inhibitory effects in bone morphogenetic protein-2- and activin A-mediated signaling in B lineage cells.
引用
收藏
页码:13637 / 13642
页数:6
相关论文
共 44 条
[31]   INDUCTION OF APOPTOSIS IN B-LINEAGE CELLS BY ACTIVIN-A DERIVED FROM MACROPHAGES [J].
NISHIHARA, T ;
OHSAKI, Y ;
UEDA, N ;
KOSEKI, T ;
ETO, Y .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 1995, 15 (06) :509-516
[32]  
PERANDONES CE, 1993, J IMMUNOL, V151, P3521
[33]   The L45 loop in type I receptors for TGF-β family members is a critical determinant in specifying Smad isoform activation [J].
Persson, U ;
Izumi, H ;
Souchelnytskyi, S ;
Itoh, S ;
Grimsby, S ;
Engström, U ;
Heldin, CH ;
Funa, K ;
ten Dijke, P .
FEBS LETTERS, 1998, 434 (1-2) :83-87
[34]   Physical and functional interaction of murine and Xenopus Smad7 with bone morphogenetic protein receptors and transforming growth factor-β receptors [J].
Souchelnytskyi, S ;
Nakayama, T ;
Nakao, A ;
Morén, A ;
Heldin, CH ;
Christian, JL ;
ten Dijke, P .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1998, 273 (39) :25364-25370
[35]   Phosphorylation of Ser(465) and Ser(467) in the C terminus of Smad2 mediates interaction with Smad4 and is required for transforming growth factor-beta signaling [J].
Souchelnytskyi, S ;
Tamaki, K ;
Engstrom, U ;
Wernstedt, C ;
tenDijke, P ;
Heldin, CH .
JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (44) :28107-28115
[36]   ADULT T-CELL LEUKEMIA - STRUCTURES AND EXPRESSION OF THE P53 GENE [J].
SUGITO, S ;
YAMATO, K ;
SAMESHIMA, Y ;
YOKOTA, J ;
YANO, S ;
MIYOSHI, I .
INTERNATIONAL JOURNAL OF CANCER, 1991, 49 (06) :880-885
[37]   Smad5 induces ventral fates in Xenopus embryo [J].
Suzuki, A ;
Chang, CB ;
Yingling, JM ;
Wang, WF ;
HemmatiBrivanlou, A .
DEVELOPMENTAL BIOLOGY, 1997, 184 (02) :402-405
[38]  
Tamaki K, 1998, J CELL PHYSIOL, V177, P355, DOI 10.1002/(SICI)1097-4652(199811)177:2<355::AID-JCP17>3.0.CO
[39]  
2-8
[40]  
TOKUNAGA K, 1987, CANCER RES, V47, P5616